首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Assembly of cartilage collagen fibrils is disrupted by overexpression of normal type II collagen in transgenic mice.
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Assembly of cartilage collagen fibrils is disrupted by overexpression of normal type II collagen in transgenic mice.

机译:正常II型胶原在转基因小鼠中的过表达破坏了软骨胶原原纤维的组装。

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摘要

Cartilage collagen fibrils, which are characterized by their thin, uniform diameters, are formed of a multicomponent system of three collagen types (II, IX, and XI) and interacting proteoglycans. We have used a genetic approach to test whether the proper assembly of this multiprotein structure was altered by overexpression of one of its normal components. Here we show that in transgenic mice in which the normal mouse alpha 1(II) collagen is overexpressed, thick abnormal collagen fibrils are generated. Mice that showed the highest expression of the transgene also displayed a larger proportion of abnormal fibrils and died at birth. We propose that an imbalance among the constituents of the cartilage collagen fibrils disrupts the mechanism that controls their assembly. The results show the applicability of the transgenic mice system to studies of complex multicomponent protein assemblies in intact animals.
机译:软骨胶原蛋白纤维的特征是细,均匀的直径,是由三种胶原蛋白类型(II,IX和XI)和相互作用的蛋白聚糖的多组分系统形成的。我们已经使用一种遗传方法来测试这种多蛋白结构的正确组装是否由于其正常成分之一的过表达而改变。在这里,我们显示在正常小鼠alpha 1(II)胶原蛋白过表达的转基因小鼠中,会产生厚厚的异常胶原蛋白原纤维。显示转基因最高表达的小鼠也显示出较大比例的异常原纤维,并在出生时死亡。我们提出,软骨胶原纤维成分之间的不平衡破坏了控制其组装的机制。结果表明,转基因小鼠系统可用于研究完整动物中复杂的多组分蛋白质装配体。

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